Active Ingredient[S]
Full Label (Complete)
American Dental
FDA Label NDC 73333-473
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nutrix International, Llc. for the product American Dental (NDC 73333-473). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient[s], purpose, use[s], warnings, do not use, when using, stop use and ask a doctor, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use[S]
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only. Flammable. Keep away from heat or flame.
Do Not Use
- On children less than 2 months of age.
- On open skin wounds
When Using
When using this product keep out of eyes, ears, mouth. In case of contact with eyes, rinse thoroughly with water.
Stop Use And Ask A Doctor
If irritation or rash occurs. These may be signs of a serious condition.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Place enough product on hands to cover all surfaces.
- Rub hands together until dry.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
- Store between 15-30°C (59-86°F)
- Avoid freezing and excessive heat above 40°C (104°F)
Inactive Ingredients
Glycerin, Hydrogen Peroxide, Purified water USP
Package
Front Label
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